MCID: IDP040
MIFTS: 11

Idiopathic Eosinophilic Myositis

Categories: Bone diseases, Neuronal diseases, Rare diseases

Aliases & Classifications for Idiopathic Eosinophilic Myositis

MalaCards integrated aliases for Idiopathic Eosinophilic Myositis:

Name: Idiopathic Eosinophilic Myositis 58
Idiopathic Eosinophilia-Associated Myopathy 58

Characteristics:

Orphanet epidemiological data:

58
idiopathic eosinophilic myositis
Inheritance: Not applicable;

Classifications:

Orphanet: 58  
Rare neurological diseases
Rare systemic and rhumatological diseases


External Ids:

ICD10 via Orphanet 33 M60.8
Orphanet 58 ORPHA247724

Summaries for Idiopathic Eosinophilic Myositis

MalaCards based summary : Idiopathic Eosinophilic Myositis, also known as idiopathic eosinophilia-associated myopathy, is related to myositis and muscular dystrophy, limb-girdle, autosomal recessive 1. An important gene associated with Idiopathic Eosinophilic Myositis is CAPN3 (Calpain 3).

Related Diseases for Idiopathic Eosinophilic Myositis

Diseases related to Idiopathic Eosinophilic Myositis via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 myositis 10.3
2 muscular dystrophy, limb-girdle, autosomal recessive 1 10.0
3 polyneuropathy 10.0
4 fibromyalgia 10.0
5 vasculitis 10.0
6 hypereosinophilic syndrome 10.0
7 calpain-3-related limb-girdle muscular dystrophy r1 10.0

Graphical network of the top 20 diseases related to Idiopathic Eosinophilic Myositis:



Diseases related to Idiopathic Eosinophilic Myositis

Symptoms & Phenotypes for Idiopathic Eosinophilic Myositis

Drugs & Therapeutics for Idiopathic Eosinophilic Myositis

Search Clinical Trials , NIH Clinical Center for Idiopathic Eosinophilic Myositis

Genetic Tests for Idiopathic Eosinophilic Myositis

Anatomical Context for Idiopathic Eosinophilic Myositis

Publications for Idiopathic Eosinophilic Myositis

Articles related to Idiopathic Eosinophilic Myositis:

# Title Authors PMID Year
1
Eosinophilic myositis as first manifestation in a patient with type 2 myotonic dystrophy CCTG expansion mutation and rheumatoid arthritis. 61
25443993 2015
2
Transcriptional explorations of CAPN3 identify novel splicing mutations, a large-sized genomic deletion and evidence for messenger RNA decay. 61
17979987 2007
3
CAPN3 mutations in patients with idiopathic eosinophilic myositis. 61
16607617 2006
4
Resolving eosinophilic myositis: MR features. 61
11176312 2001
5
Idiopathic eosinophilic myositis associated with vasculitis and symmetrical polyneuropathy. 61
9133947 1997
6
Idiopathic eosinophilic myositis. 61
7648245 1995
7
Idiopathic eosinophilic myositis with preexisting fibromyalgia. 61
3981504 1985

Variations for Idiopathic Eosinophilic Myositis

Expression for Idiopathic Eosinophilic Myositis

Search GEO for disease gene expression data for Idiopathic Eosinophilic Myositis.

Pathways for Idiopathic Eosinophilic Myositis

GO Terms for Idiopathic Eosinophilic Myositis

Sources for Idiopathic Eosinophilic Myositis

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
20 GARD
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
53 NINDS
54 Novoseek
56 OMIM via Orphanet
57 OMIM® (Updated 05-Apr-2021)
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 Tocris
70 UMLS
71 UMLS via Orphanet
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